tert-butyl 4-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate

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To solve the problem of this chemical structure, it is necessary to analyze it in detail. Fufuran group is a group with a specific cyclic structure, rich in hydrocarbons, and its unique shape and properties are also unique. And 4-oxo octa-hydrocyclopenta [c] pyrrole-2 (1H) -carboxylic acid amide, this title contains complex chemical structure information.
First look at its main frame, octa-hydrocyclopenta [c] pyrrole, which is a multi-ring system formed by the fusing of cyclopentane and pyrrole ring. After eight hydrogenations, the double bonds in the ring are mostly saturated, and the structure tends to be stable. " 4-Oxo ", shown at position 4 of cyclopentyl pyrrole structure, with a carbonyl group. The presence of this carbonyl group significantly affects the chemical activity and physical properties of the compound. Carbonyl groups have strong electron-absorbing properties, which can change the density of surrounding electron clouds and affect the reactivity of connected atoms.
Furthermore," 2 (1H) -carboxylic acid amide "indicates that at position 2, there is a carboxylic acid amide group related to 1H. Carboxylic acid amide is formed by the condensation of carboxyl and amino groups, and has the properties of both carboxylic and amino groups. The introduction of this group endows the compound with certain polarity and reaction check points. The properties of amide bonds enable it to undergo hydrolysis, condensation and other reactions under certain conditions.
Overall, the structure of this compound is complex and delicate, and the interaction and synergy of various groups give it unique chemical properties and potential application value. Its structure includes both stable multi-cyclic skeletons and active carbonyl and amide groups, which may be of important research significance in the fields of organic synthesis and drug development.

Fupentyl and 4-oxo-octahydrocyclooctene [C] to spiro-2 (1H) -naphthalic anhydride, its main use is particularly important.
amyl derivatives are often used in organic synthesis as key structural units. When creating complex organic molecules, amyl groups can be introduced through various chemical reactions, such as alkylation, acylation, etc., to shape the specific configuration and characteristics of the molecule, in order to meet the needs of drug development, materials science and other fields.
As for 4-oxo-octahydrocyclooctene [C] trospiro-2 (1H) -naphthalic anhydride, it is of great potential value in the field of medicinal chemistry. Its unique chemical structure may endow the drug with unique biological activity and targeting. It can be used as the core structure of the lead compound, modified and optimized to find new drugs with high efficiency and low toxicity.
In the field of materials science, such compounds may be specially treated to prepare materials with special optical, electrical or mechanical properties. For example, by polymerizing and introducing it into a polymer system, it is expected to improve the properties of the material for use in special scenarios. < Br >
And because of its structure, it can be used as a unique catalyst or ligand in the field of organic catalysis, which can help the efficient and high selectivity of catalytic reactions and promote the development of organic synthetic chemistry.
These two are indispensable in many fields such as organic synthesis, drug development, materials science and organic catalysis, and are the key to chemical research and application.

To prepare ethyl furano [C] pyrrole-2 (1H) -carboxylate, there are various methods. Looking at the method of "Tiangong Kaiwu", although it does not directly refer to this, the idea of its creation may be the way to go.
First, the conventional path of organic synthesis can be followed. Using the raw material containing furan and pyrrole structures as the base, the method of functional group transformation is used. For example, first take a suitable furan derivative, make it and a nitrogen-containing nucleophilic reagent, at the right temperature and pressure and when there is a catalyst, carry out a nucleophilic substitution reaction to form a pyrrole ring at the beginning. After oxidation, esterification and other steps, the target furo [C] pyrrole-2 (1H) -carboxylic acid ethyl ester is obtained. Among them, the oxidation step requires careful selection of reagents and conditions to prevent excessive oxidation from causing product damage. During esterification, the ratio of acid to alcohol, temperature and catalyst dosage should also be adjusted to increase the yield.
Second, it can be led by the method of reverse synthesis analysis. The target product is disassembled in reverse, and what kind of intermediates can be obtained by what reaction. Or disassembled into furan fragments and pyrrole fragments, respectively, and then spliced. For example, the active intermediate of furan is first prepared, and then the key intermediate of pyrrole is reacted with it. This requires detailed examination of the activity and reactivity of the fragment, so that the two can be connected smoothly and avoid side reactions.
Third, we can refer to the theory of biomimetic synthesis. Observe the mechanism of the formation of substances containing such structures in nature, and simulate the process of biological enzyme catalysis. Although the biological system is complex, the key steps are extracted and imitated by chemical means. For example, find a catalyst similar to the active center of biological enzymes, imitate its efficient catalysis under mild conditions, so that the reaction can be carried out in a more suitable environment, or increase the selectivity and yield of the reaction to obtain pure furano [C] pyrrole-2 (1H) -carboxylate ethyl ester.

Fufuryl-4-oxo-octahydrocyclopenta [c] pyrrole-2 (1H) -carboxylic acid ester is a kind of organic compound. Its physical properties are quite characteristic.
Looking at its form, it often exists in the world as a solid state, which is due to the force between molecules. Molecules attract each other, causing them to be closely arranged, so they form a solid state.
As for the color, it is mostly white or off-white. The formation of this color is related to the transition of electrons in the molecular structure. Its structure makes electrons transition between specific energy levels, absorb and reflect light of specific wavelengths, so it appears this color.
When it comes to melting point, there is a specific value due to the regularity of molecular structure and the magnitude of intermolecular forces. If the intermolecular forces are strong, more energy is required to destroy the lattice structure, and the melting point is high; otherwise, it is low.
In terms of solubility, it has a certain solubility in organic solvents, such as ethanol and acetone. Because the molecule of the compound has a certain polarity, hydrogen bonds or other intermolecular forces can be formed with the molecules of the organic solvent, so it can be dissolved. However, the solubility in water is relatively limited, because the polarity of the water molecule and the molecular polarity of the compound are not perfectly matched, and the interaction is weak.
And its density is also one end of its physical properties. The density depends on the molecular mass and the way the molecules are packed, reflecting the mass distribution in a unit volume.
All these physical properties are closely related to the molecular structure of the compound, and the structure determines the properties. This is a principle of chemistry.

What is the future of fufuzazo [C] pyrazole-2 (1H) -carboxylic acid esters? This is a key question in the field of chemistry. Looking at "Tiangong Kaiwu", although it does not deal with this specific compound in detail, it has insights into the properties, uses and systems of matter, and can be explored by analogy.
Fufuzazo [C] pyrazole-2 (1H) -carboxylic acid esters contain unique fuzazo and pyrazole structures, which may endow them with specific chemical properties. From the perspective of chemical synthesis, its preparation may be challenging, requiring exquisite skills and suitable reagents. If the synthesis problem can be overcome, this compound may emerge in many fields.
In the field of medicine, due to its special structure or specific combination with biological targets, it has the potential to become a new type of drug lead compound. It can be used to develop antibacterial, antiviral or anti-tumor drugs for human health and well-being. However, in order to achieve this, rigorous pharmacological experiments and clinical trials are required to prove its safety and effectiveness.
In materials science, or due to the stability and functionality endowed by the structure, it is suitable for the development of high-performance materials. Such as preparing special coating materials to enhance the corrosion resistance and wear resistance of materials; or for synthesizing optoelectronic materials to regulate the characteristics of light absorption and emission.
However, its prospects also pose challenges. Synthetic costs may be high, limiting large-scale production and application. And the understanding of its environmental impact is still shallow, and in-depth research is needed to ensure environmental friendliness.
In short, furazo [C] pyrazole-2 (1H) -carboxylate has a bright future, but it also needs researchers to make unremitting efforts to overcome problems such as synthesis, cost, and environment in order to give full play to its potential and benefit mankind.